Antibody response dynamics to CoronaVac vaccine and booster immunization in adults and the elderly: A long-term, longitudinal prospective study.

COVID-19 COVID-19 vaccine booster shot CoronaVac vaccine Humoral Immunity

Journal

IJID regions
ISSN: 2772-7076
Titre abrégé: IJID Reg
Pays: England
ID NLM: 9918418183106676

Informations de publication

Date de publication:
Jun 2023
Historique:
received: 06 01 2023
revised: 27 03 2023
accepted: 03 04 2023
medline: 27 4 2023
pubmed: 27 4 2023
entrez: 27 4 2023
Statut: ppublish

Résumé

The long-term humoral immune response after vaccination varies between vaccines and is dependent on the accuracy of the antibody test. A better understanding of the vaccine immune response may help to define vaccination strategies against coronavirus disease 2019 (COVID-19). To investigate the long-term immunological response to CoronaVac vaccine and determinants of breakthrough COVID-19 infection. A long-term, prospective cohort study involving vaccinated adult and elderly subjects was conducted to investigate the presence of anti-RBD-specific immunoglobulin (Ig)G, anti-nucleocapsid IgG and anti-spike trimeric protein IgG. Antibody level dynamics and risk factors associated with breakthrough COVID-19 infection were investigated. In total, 3902 participants were included in this study. Vaccination with two doses of CoronaVac and a booster dose increased the levels of anti-RBD-specific IgG, anti-nucleocapsid IgG and anti-spike trimeric IgG significantly. In adults, anti-nucleocapsid IgG and anti-spike trimeric IgG levels decreased significantly 7 months after the second dose. In adults and the elderly, the levels of anti-spike trimeric IgG and anti-RBD IgG decreased significantly 4 and 6 months after the booster dose, respectively. Previous exposure to severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) and anti-spike trimeric IgG titres was independently associated with a lower probability of post-vaccination infection. A significant increase in antibody levels was found after two doses of CoronaVac and a booster dose. Antibody titres declined significantly 7 months post-vaccination in participants who did not receive a booster dose. Higher levels of antibodies and previous SARS-CoV-2 infection were associated with protection against breakthrough COVID-19.

Sections du résumé

Background UNASSIGNED
The long-term humoral immune response after vaccination varies between vaccines and is dependent on the accuracy of the antibody test. A better understanding of the vaccine immune response may help to define vaccination strategies against coronavirus disease 2019 (COVID-19).
Objective UNASSIGNED
To investigate the long-term immunological response to CoronaVac vaccine and determinants of breakthrough COVID-19 infection.
Methods UNASSIGNED
A long-term, prospective cohort study involving vaccinated adult and elderly subjects was conducted to investigate the presence of anti-RBD-specific immunoglobulin (Ig)G, anti-nucleocapsid IgG and anti-spike trimeric protein IgG. Antibody level dynamics and risk factors associated with breakthrough COVID-19 infection were investigated.
Results UNASSIGNED
In total, 3902 participants were included in this study. Vaccination with two doses of CoronaVac and a booster dose increased the levels of anti-RBD-specific IgG, anti-nucleocapsid IgG and anti-spike trimeric IgG significantly. In adults, anti-nucleocapsid IgG and anti-spike trimeric IgG levels decreased significantly 7 months after the second dose. In adults and the elderly, the levels of anti-spike trimeric IgG and anti-RBD IgG decreased significantly 4 and 6 months after the booster dose, respectively. Previous exposure to severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) and anti-spike trimeric IgG titres was independently associated with a lower probability of post-vaccination infection.
Conclusions UNASSIGNED
A significant increase in antibody levels was found after two doses of CoronaVac and a booster dose. Antibody titres declined significantly 7 months post-vaccination in participants who did not receive a booster dose. Higher levels of antibodies and previous SARS-CoV-2 infection were associated with protection against breakthrough COVID-19.

Identifiants

pubmed: 37102137
doi: 10.1016/j.ijregi.2023.04.003
pii: S2772-7076(23)00045-0
pmc: PMC10076246
doi:

Types de publication

Journal Article

Langues

eng

Pagination

222-229

Informations de copyright

© 2023 The Author(s).

Déclaration de conflit d'intérêts

MCB, GJV, NNF, PMMG, GRM, BALF and RTC received research support from Instituto Butantan during the conduct of this study. SCSV, LBS, MAALSA, PEB, SK, HABG, JDF, MAL, PHMP and DTC are employees of Instituto Butantan.

Références

Rev Med Virol. 2021 May;31(3):e2181
pubmed: 33152146
Nature. 2021 Aug;596(7872):417-422
pubmed: 34192737
Clin Infect Dis. 2023 Feb 8;76(3):e299-e307
pubmed: 35675370
Lancet Infect Dis. 2022 Jan;22(1):56-63
pubmed: 34509185
N Engl J Med. 2021 Dec 9;385(24):e84
pubmed: 34614326
Lancet Reg Health Eur. 2021 Nov;10:100208
pubmed: 34514454
Public Health Pract (Oxf). 2022 Dec;4:100301
pubmed: 35946045
Lancet Infect Dis. 2021 Feb;21(2):181-192
pubmed: 33217362
Sci Rep. 2021 Feb 10;11(1):3455
pubmed: 33568776
J Allergy Clin Immunol. 2020 May;145(5):1309-1321
pubmed: 32386655
Trials. 2020 Oct 15;21(1):853
pubmed: 33059771
Lancet. 2022 Mar 5;399(10328):924-944
pubmed: 35202601
Clin Infect Dis. 2021 Dec 6;73(11):2065-2072
pubmed: 33906236
Nature. 2021 Dec;600(7890):701-706
pubmed: 34673755
Lancet Infect Dis. 2021 Jun;21(6):803-812
pubmed: 33548194
Clin Infect Dis. 2023 Feb 8;76(3):e360-e366
pubmed: 35639918
Lancet Respir Med. 2021 Nov;9(11):e104-e105
pubmed: 34687656
Lancet. 2021 Jul 17;398(10296):213-222
pubmed: 34246358
Science. 2022 Jan 07;375(6576):43-50
pubmed: 34812653
J Virol. 2021 Jan 13;95(3):
pubmed: 33144321
Nat Commun. 2020 Jul 14;11(1):3581
pubmed: 32665645
Lancet Infect Dis. 2020 May;20(5):533-534
pubmed: 32087114
Clin Chem Lab Med. 2021 Mar 15;59(8):1463-1467
pubmed: 33711225
Rheumatol Int. 2021 Aug;41(8):1429-1440
pubmed: 34109466
BMJ. 2022 Mar 2;376:e068632
pubmed: 35236664
Lancet Infect Dis. 2020 Aug;20(8):e192-e197
pubmed: 32539990
BMC Med. 2022 Jun 9;20(1):216
pubmed: 35676738
Nat Med. 2021 Jul;27(7):1205-1211
pubmed: 34002089
J Clin Virol. 2020 Aug;129:104512
pubmed: 32563180
BMJ. 2020 Jul 1;370:m2516
pubmed: 32611558
Expert Rev Vaccines. 2022 Aug;21(8):1071-1086
pubmed: 35604776

Auteurs

Gustavo Jardim Volpe (GJ)

Serrana State Hospital, Serrana, São Paulo, Brazil.

Sandra Coccuzzo Sampaio Vessoni (SCS)

Instituto Butantan, São Paulo, São Paulo, Brazil.

Lais Braga Soares (LB)

Fundação Butantan, São Paulo, São Paulo, Brazil.

Maria Aparecida Alves Leite Dos Santos Almeida (MAA)

Fundação Butantan, São Paulo, São Paulo, Brazil.

Patrícia Emília Braga (PE)

Fundação Butantan, São Paulo, São Paulo, Brazil.

Glenda Renata de Moraes (GR)

Health Department, Serrana, São Paulo, Brazil.

Natasha Nicos Ferreira (NN)

Serrana State Hospital, Serrana, São Paulo, Brazil.

Pedro Manoel Marques Garibaldi (PMM)

Serrana State Hospital, Serrana, São Paulo, Brazil.

Simone Kashima (S)

Ribeirão Preto Medical School, University of São Paulo, Ribeirão Preto, São Paulo, Brazil.

Benedito Antônio Lopes Fonseca (BAL)

Ribeirão Preto Medical School, University of São Paulo, Ribeirão Preto, São Paulo, Brazil.

Rodrigo Tocantins Calado (RT)

Ribeirão Preto Medical School, University of São Paulo, Ribeirão Preto, São Paulo, Brazil.

Hugo Alberto Brango García (HAB)

Departamento de Matemáticas y Estadística, Universidad del Norte, Barranquilla, Colombia.

João Italo Dias de França (JID)

Fundação Butantan, São Paulo, São Paulo, Brazil.

Marcos Alves de Lima (MA)

Fundação Butantan, São Paulo, São Paulo, Brazil.

Pedro Henrique de Mesquita Pacheco (PHM)

Fundação Butantan, São Paulo, São Paulo, Brazil.

Marcos Carvalho Borges (MC)

Serrana State Hospital, Serrana, São Paulo, Brazil.
Ribeirão Preto Medical School, University of São Paulo, Ribeirão Preto, São Paulo, Brazil.

Dimas Tadeu Covas (DT)

Instituto Butantan, São Paulo, São Paulo, Brazil.

Classifications MeSH